intuitive assembly instructions rely heavily on images to convey information. by generating configurable, true to life assemblies, designPORT is able to quickly and easily produce stylized images to communicate with minimal verbiage the steps and equipment necessary to assemble complex products.

assembly and inspection procedure for medical devices requires methodical documentation and verification. to support this, designPORT used large color images from CAD models along with photographs to create detailed instructions outlining assembly, inspection, and safety procedure for an entire product line. obvious color coding and other visual cues were used to ensure proper execution by assembly line workers.

developing detailed drawings and bills of materials for every part and sub-assembly in your product line can be a daunting, yet essential task. our team of engineers understands and is ready to help by taking your product or prototype and generating a complete document outlining critical and inspection dimensions, geometric tolerances and bills of materials. This type of detailed documentation not only streamlines communication with vendors but also creates a medium for holding them accountable for keeping parts and assemblies within spec.

to build an entire product line with a single model, designPORT constructed a sophisticated, design table driven part. research and analysis was done to determine proper sizing for standard wire and pipe gauges, as well as logical size ranges for each part to maximize marketability. this combination of methodical design and sophisticated 3D modeling allowed designPORT to deliver to our clients a well structured product line contained within a single file.

given rough 2D drawings, designPORT created manufacturable, prototype ready designs. these complex wheel assemblies were analyzed to maximize manufacturability and control tolerance stack throughout. the end product was a full set of 3D models and detail drawings that allowed our client to move independently through prototype validation then on to seek out manufacturing facilities for production.